Canonical Allele Identifier: CA4881055

Gene: DNAAF11

Linked Data

• dbSNP Id: rs369472078
• ExAC: 8:133584503 A / G
• gnomAD v2: 8-133584503-A-G
• gnomAD v3: 8-132572255-A-G
• gnomAD v4: 8-132572255-A-G
• MyVariant Identifiers: chr8:g.133584503A>G (hg19) ; chr8:g.132572255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572255A>G , CM000670.2:g.132572255A>G	GRCh38
NC_000008.10:g.133584503A>G , CM000670.1:g.133584503A>G	GRCh37
NC_000008.9:g.133653685A>G	NCBI36
NG_033068.1:g.108361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*51T>C MANE Select	ENSP00000484634.1:n.*51T>C
ENST00000250173.5:c.*316T>C	ENSP00000250173.2:n.*316T>C
ENST00000518642.5:c.*316T>C	ENSP00000428610.1:n.*316T>C
ENST00000519595.5:c.*51T>C	ENSP00000429791.1:n.*51T>C
ENST00000522789.5:c.672T>C	ENSP00000428015.1:n.672T>C
ENST00000618342.1:c.1452T>C	ENSP00000484802.1:n.1452T>C
ENST00000620350.4:c.*51T>C	ENSP00000484634.1:n.*51T>C
NM_012472.4:c.*51T>C	NP_036604.2:n.*51T>C
NR_073525.1:n.1676T>C
XM_006716538.2:c.*51T>C	XP_006716601.2:n.*51T>C
XM_011516950.1:c.*51T>C	XP_011515252.1:n.*51T>C
XM_011516952.1:c.*51T>C	XP_011515254.1:n.*51T>C
XM_011516953.1:c.*51T>C	XP_011515255.1:n.*51T>C
XM_011516954.1:c.*51T>C	XP_011515256.1:n.*51T>C
XR_428377.2:n.1704T>C
NM_001321961.1:c.*51T>C	NP_001308890.1:n.*51T>C
NM_001321962.1:c.*51T>C	NP_001308891.1:n.*51T>C
NM_001321963.1:c.*51T>C	NP_001308892.1:n.*51T>C
NM_001321964.1:c.*51T>C	NP_001308893.1:n.*51T>C
NM_001321965.1:c.*51T>C	NP_001308894.1:n.*51T>C
NM_001321966.1:c.*51T>C	NP_001308895.1:n.*51T>C
NM_012472.5:c.*51T>C	NP_036604.2:n.*51T>C
NR_073525.2:n.1676T>C
NR_135905.1:n.1665T>C
NR_135906.1:n.1106T>C
NR_135907.1:n.1352T>C
NR_135908.1:n.1046T>C
NR_135909.1:n.1470T>C
NR_135910.1:n.1777T>C
NR_135911.1:n.1856T>C
NR_135912.1:n.2415T>C
NR_135913.1:n.2102T>C
XM_006716538.3:c.*51T>C	XP_006716601.2:n.*51T>C
XM_011516950.2:c.*51T>C	XP_011515252.1:n.*51T>C
XM_017013296.1:c.*51T>C	XP_016868785.1:n.*51T>C
XM_017013297.1:c.*51T>C	XP_016868786.1:n.*51T>C
XM_017013298.1:c.*51T>C	XP_016868787.1:n.*51T>C
NM_012472.6:c.*51T>C MANE Select	NP_036604.2:n.*51T>C
NM_001321961.2:c.*51T>C	NP_001308890.1:n.*51T>C
NM_001321962.2:c.*51T>C	NP_001308891.1:n.*51T>C
NM_001321963.2:c.*51T>C	NP_001308892.1:n.*51T>C
NM_001321964.2:c.*51T>C	NP_001308893.1:n.*51T>C
NM_001321965.2:c.*51T>C	NP_001308894.1:n.*51T>C
NM_001321966.2:c.*51T>C	NP_001308895.1:n.*51T>C
NR_073525.3:n.1604T>C
NR_135905.2:n.1593T>C
NR_135906.2:n.1034T>C
NR_135907.2:n.1280T>C
NR_135908.2:n.974T>C
NR_135909.2:n.1490T>C
NR_135910.2:n.1840T>C
NR_135911.2:n.1960T>C
NR_135912.2:n.2519T>C
NR_135913.2:n.2206T>C